Ramachandran Balaji, Rizzi Nicoletta, Maggi Adriana
Center of Excellence on Neurodegenerative Diseases and Department of Pharmacological Sciences, University of Milan Via Balzaretti, 9 I-20123 Milan, Italy.
Center of Excellence on Neurodegenerative Diseases and Department of Pharmacological Sciences, University of Milan Via Balzaretti, 9 I-20123 Milan, Italy ; Animal Models Platform Fondazione Filarete Milan, Italy.
Am J Nucl Med Mol Imaging. 2014 Apr 25;4(3):270-82. eCollection 2014.
CdCl2 salt is widely used in exposure oriented studies, while the biological exposure of Cadmium (Cd) occurs mostly through diet. Hence, we designed a in vivo imaging methodology with sexually immature male ERE-Luc reporter mice to test the estrogen-like (EL) effects of Cd as a natural component in wheat and flax bread based diets (containing 17.57 and 49.22 ug/kg Cd concentrations respectively) and CdCl2 per-oral dose of 1 ug/kg/bw/day. Total exposure of ingested and % bioaccumulation of Cd in selected organs were estimated as 547 ng (4.4%), 776 ng (0.3%) and 2131.8 ng (0.1%) corresponding to CdCl2, wheat and flax bread based diet treatments respectively. Cd from CdCl2 bioaccumulated more readily, despite the exposure of Cd is higher with bread based diets. Longitudinal in vivo imaging did not reveal significant changes in luciferase activity. White adipose tissue (WAT) and prostate were identified as novel target organs of Cd. Indeed, the rest of the observed EL effects, endogenous target gene expression and necropsy findings are not consistent to any particular organ or treatment. This implies that, the observed EL effects due to low doses of Cd (either from CdCl2 or dietary form) occur only as subtle changes at the molecular level, but inadequate to cause significant changes at the anatomo-pathological level during the 21 day exposure period. The study demonstrates the sensitivity of the methodology to assess EL effects of food embedded Cd and underlines the limitations of directly extrapolating the results of suspected chemicals in their pure form to dietary exposure scenarios.
氯化镉盐广泛应用于面向暴露的研究中,而镉(Cd)的生物暴露主要通过饮食发生。因此,我们设计了一种体内成像方法,使用性未成熟的雄性ERE-Luc报告基因小鼠,以测试镉作为小麦和亚麻籽面包基础饮食(分别含有17.57和49.22微克/千克镉浓度)中的天然成分以及每天每千克体重口服1微克氯化镉剂量时的雌激素样(EL)效应。估计摄入的镉总量以及选定器官中镉的生物累积百分比分别为547纳克(4.4%)、776纳克(0.3%)和2131.8纳克(0.1%),分别对应氯化镉、小麦和亚麻籽面包基础饮食处理。尽管基于面包的饮食中镉的暴露量更高,但来自氯化镉的镉更容易生物累积。纵向体内成像未显示荧光素酶活性有显著变化。白色脂肪组织(WAT)和前列腺被确定为镉的新靶器官。事实上,观察到的其他EL效应、内源性靶基因表达和尸检结果与任何特定器官或处理均不一致。这意味着,低剂量镉(来自氯化镉或饮食形式)所观察到的EL效应仅在分子水平上表现为细微变化,但在21天的暴露期内不足以在解剖病理学水平上引起显著变化。该研究证明了该方法评估食物中嵌入镉的EL效应的敏感性,并强调了将疑似化学物质纯形式的结果直接外推到饮食暴露场景的局限性。